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1.
Int J Nanomedicine ; 13: 3081-3091, 2018.
Article in English | MEDLINE | ID: mdl-29872295

ABSTRACT

BACKGROUND: Anticaries agents must interfere with the adhesion of Streptococcus mutans and its proliferation in dental biofilm, without causing host toxicity and bacterial resistance. Natural substances, including cationic antimicrobial peptides (CAMPs) and their fragments, such as ß-defensin-3 peptide fragment (D1-23), have been widely studied. However, the chemical and physical stability of CAMPs may be compromised by external factors, such as temperature and pH, reducing the period of antimicrobial activity. METHODS: To overcome the aforementioned disadvantage, this study developed and character-ized a drug delivery system and evaluated the cytotoxicity and effect against S. mutans biofilm of a D1-23-loaded bioadhesive liquid crystalline system (LCS). LCS was composed of oleic acid, polyoxypropylene-(5)-polyoxyethylene-(20)-cetyl alcohol, Carbopol® 974P and Carbopol® 971P. LCS was analyzed by polarized light microscopy (PLM), rheology (viscoelasticity and flow properties) and in vitro bioadhesion. The viability of epithelial cells was evaluated. Minimal inhibitory concentration (MIC) and minimal bactericidal concentration (MBC) against S. mutans were determined for D1-23 for further evaluation of the effect against S. mutans biofilm after 4 and 24 h of exposure to treatments. RESULTS: PLM, rheology, and in vitro bioadhesion tests showed that both viscosity and bioadhesion of LCS increased after it was diluted with artificial saliva. D1-23-loaded LCS system presented better activity against S. mutans biofilm after 24 h when compared to 4 h of treatment, showing a cumulative effect. Neither LCS nor D1-23-loaded LCS presented toxicity on human epithelial cells. CONCLUSION: D1-23-loaded LCS is a promising drug delivery system for the prevention of dental caries.


Subject(s)
Anti-Bacterial Agents/administration & dosage , Antimicrobial Cationic Peptides/administration & dosage , Dental Caries/prevention & control , Drug Delivery Systems/methods , Streptococcus mutans/drug effects , Acrylates/chemistry , Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/pharmacology , Antimicrobial Cationic Peptides/chemistry , Antimicrobial Cationic Peptides/pharmacology , Biofilms/drug effects , Cell Line , Dental Caries/microbiology , Dental Cements/chemistry , Epithelial Cells/drug effects , Humans , Liquid Crystals/chemistry , Microbial Sensitivity Tests , Streptococcus mutans/pathogenicity , Streptococcus mutans/physiology , beta-Defensins/chemistry
2.
Braz. dent. j ; 28(3): 317-323, May-June 2017. tab, graf
Article in English | LILACS | ID: biblio-888643

ABSTRACT

Abstract The aim of this study was to evaluate the surface free energy (SFE), wetting and surface properties as well as antimicrobial, adhesion and biocompatibility properties of diamond-like carbon (DLC)-coated surfaces. In addition, the leakage of Escherichia coli through the abutment-dental implant interface was also calculated. SFE was calculated from contact angle values; R a was measured before and after DLC coating. Antimicrobial and adhesion properties against E. coli and cytotoxicity of DLC with human keratinocytes (HaCaT) were evaluated. Further, the ability of DLC-coated surfaces to prevent the migration of E. coli into the external hexagonal implant interface was also evaluated. A sterile technique was used for the semi-quantitative polymerase chain reaction (semi-quantitative PCR). The surfaces showed slight decreases in cell viability (p<0.05), while the SFE, R a, bacterial adhesion, antimicrobial, and bacterial infiltration tests showed no statistically significant differences (p>0.05). It was concluded that DLC was shown to be a biocompatible material with mild cytotoxicity that did not show changes in R a, SFE, bacterial adhesion or antimicrobial properties and did not inhibit the infiltration of E. coli into the abutment-dental implant interface.


Resumo O objetivo deste trabalho foi avaliar a energia livre de superfície (ELS), molhabilidade e propriedades de superfície assim como propriedades antimicrobianas, de adesão e biocompatibilidade de superfícies recobertas com Diamond-Like Carbon (DLC). Além disso, investigou-se a infiltração de Escherichia coli por meio da interface abutment-implante dentário. ELS foi calculada a partir dos valores de ângulo de contato; Ra foi medida antes e depois do revestimento com DLC. Foram avaliadas propriedades antimicrobianas e de adesão contra E. coli e citotoxicidade do DLC utilizando queratinócitos humanos (HaCaT). Além disso, também avaliamos a capacidade para impedir a migração de E. coli na interface do implante hexágono externo. Uma técnica estéril foi utilizada para a reação em cadeia da polimerase semi-quantitativa (PCR semi-quantitativo). As superfícies mostraram uma ligeira diminuição da viabilidade celular (p<0,05), enquanto a ELS, R a , adesão bacteriana, testes antimicrobianos e de infiltração não apresentaram diferenças estatisticamente significativas (p>0,05). Concluiu-se que o DLC demonstrou ser um material biocompatível levemente citotóxico que não mostra alterações na Ra , ELS, adesão bacteriana ou propriedades antimicrobianas e não inibiu a infiltração de E. coli na interface abutment-implante dentário.


Subject(s)
Humans , Biofilms , Carbon , Coated Materials, Biocompatible , Dental Abutments , Dental Implants , Diamond , Anti-Bacterial Agents , Bacterial Adhesion , Cell Line , Escherichia coli/isolation & purification , Escherichia coli/physiology , Keratinocytes/cytology , Polymerase Chain Reaction , Surface Properties
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